NDUFS6 Gene Mitochondrial complex I deficiency Genetic Test
Test Name: NDUFS6 Gene Mitochondrial complex I deficiency Genetic Test
Components: NGS Technology
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Test Type: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for NDUFS6 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS6 Gene Mitochondrial complex I deficiency.
Test Details
NDUFS6 gene mitochondrial complex I deficiency is a rare genetic disorder that affects the function of complex I in the mitochondria. Complex I is responsible for the first step in the electron transport chain, which is crucial for energy production in the body.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variations in the NDUFS6 gene that may be responsible for the disorder.
The NGS genetic test involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the DNA to identify any changes in the NDUFS6 gene. These changes can include mutations, deletions, or insertions that may disrupt the normal function of the gene and lead to mitochondrial complex I deficiency.
The results of the NGS genetic test can help diagnose mitochondrial complex I deficiency and provide valuable information for healthcare providers to develop a treatment plan. Additionally, genetic testing can also provide information about the inheritance pattern of the disorder, which can be useful for family planning and genetic counseling.
| Test Name | NDUFS6 Gene Mitochondrial complex I deficiency Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for NDUFS6 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS6 Gene Mitochondrial complex I deficiency |
| Test Details |
NDUFS6 gene mitochondrial complex I deficiency is a rare genetic disorder that affects the function of complex I in the mitochondria. Complex I is responsible for the first step in the electron transport chain, which is crucial for energy production in the body. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variations in the NDUFS6 gene that may be responsible for the disorder. The NGS genetic test involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the DNA to identify any changes in the NDUFS6 gene. These changes can include mutations, deletions, or insertions that may disrupt the normal function of the gene and lead to mitochondrial complex I deficiency. The results of the NGS genetic test can help diagnose mitochondrial complex I deficiency and provide valuable information for healthcare providers to develop a treatment plan. Additionally, genetic testing can also provide information about the inheritance pattern of the disorder, which can be useful for family planning and genetic counseling. |
